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rs12144939

From SNPedia

Orientationplus
Stabilizedplus
Make rs12144939(G;G)
Make rs12144939(G;T)
Make rs12144939(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196729815
GeneCFH
is asnp
is mentioned by
dbSNPrs12144939
ebirs12144939
HLIrs12144939
Exacrs12144939
Varsomers12144939
Maprs12144939
PheGenIrs12144939
hapmaprs12144939
1000 genomesrs12144939
hgdprs12144939
ensemblrs12144939
gopubmedrs12144939
geneviewrs12144939
scholarrs12144939
googlers12144939
pharmgkbrs12144939
gwascentralrs12144939
openSNPrs12144939
23andMers12144939
23andMe allrs12144939
SNP Nexus

SNPshotrs12144939
SNPdbers12144939
MSV3drs12144939
GWAS Ctlgrs12144939
GMAF0.1905
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 21882633] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]

[PMID 24675670OA-icon.png] Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels